全文获取类型
收费全文 | 1757篇 |
免费 | 229篇 |
专业分类
1986篇 |
出版年
2022年 | 18篇 |
2021年 | 37篇 |
2020年 | 14篇 |
2019年 | 16篇 |
2018年 | 18篇 |
2017年 | 16篇 |
2016年 | 36篇 |
2015年 | 66篇 |
2014年 | 68篇 |
2013年 | 86篇 |
2012年 | 105篇 |
2011年 | 118篇 |
2010年 | 77篇 |
2009年 | 73篇 |
2008年 | 100篇 |
2007年 | 105篇 |
2006年 | 88篇 |
2005年 | 100篇 |
2004年 | 83篇 |
2003年 | 80篇 |
2002年 | 88篇 |
2001年 | 55篇 |
2000年 | 38篇 |
1999年 | 35篇 |
1998年 | 26篇 |
1997年 | 15篇 |
1996年 | 19篇 |
1995年 | 11篇 |
1994年 | 17篇 |
1993年 | 20篇 |
1992年 | 25篇 |
1991年 | 19篇 |
1990年 | 25篇 |
1989年 | 19篇 |
1988年 | 16篇 |
1987年 | 31篇 |
1986年 | 19篇 |
1985年 | 20篇 |
1984年 | 16篇 |
1983年 | 11篇 |
1982年 | 15篇 |
1981年 | 13篇 |
1980年 | 8篇 |
1979年 | 9篇 |
1978年 | 7篇 |
1977年 | 11篇 |
1976年 | 6篇 |
1975年 | 8篇 |
1974年 | 13篇 |
1973年 | 7篇 |
排序方式: 共有1986条查询结果,搜索用时 15 毫秒
1.
Three Approaches to the Study of Language and Gender 总被引:1,自引:0,他引:1
Bonnie McElhinny 《American anthropologist》2003,105(4):848-852
Gender across Languages: The Linguistic Representation of Women and Men. Vol. 2. Marlis Hellinger and Hadumod Bußmann eds. Amsterdam: John Benjamins, 2002. 348 pp.
Gender Identity and Discourse Analysis. Lia Litosseliti and Jane Sunderland eds. Amsterdam: John Benjamins, 2002. 335 pp.
Talking Gender and Sexuality. Paul McIlvenny. ed. Amsterdam: John Benjamins, 2002. 327 pp. 相似文献
Gender Identity and Discourse Analysis. Lia Litosseliti and Jane Sunderland eds. Amsterdam: John Benjamins, 2002. 335 pp.
Talking Gender and Sexuality. Paul McIlvenny. ed. Amsterdam: John Benjamins, 2002. 327 pp. 相似文献
2.
Melinda Bonnie Fagan 《Biology & philosophy》2012,27(2):179-213
Stem cell biology and systems biology are two prominent new approaches to studying cell development. In stem cell biology,
the predominant method is experimental manipulation of concrete cells and tissues. Systems biology, in contrast, emphasizes
mathematical modeling of cellular systems. For scientists and philosophers interested in development, an important question
arises: how should the two approaches relate? This essay proposes an answer, using the model of Waddington’s landscape to
triangulate between stem cell and systems approaches. This simple abstract model represents development as an undulating surface
of hills and valleys. Originally constructed by C. H. Waddington to visually explicate an integrated theory of genetics, development
and evolution, the landscape model can play an updated unificatory role. I examine this model’s structure, representational
assumptions, and uses in all three contexts, and argue that explanations of cell development require both mathematical models
and concrete experiments. On this view, the two approaches are interdependent, with mathematical models playing a crucial
but circumscribed role in explanations of cell development. 相似文献
3.
4.
5.
Maria A. Papathanasopoulos Francois Krier Anne-Marie Revol-Junelles Gerard Lefebvre Jean Pierre Le Caer Alexander von Holy John W. Hastings 《Current microbiology》1997,35(6):331-335
Leuconostoc (Lc.) mesenteroides TA33a produced three bacteriocins with different inhibitory activity spectra. Bacteriocins were purified by adsorption/desorption
from producer cells and reverse phase high-performance liquid chromatography. Leucocin C-TA33a, a novel bacteriocin with a
predicted molecular mass of 4598 Da, inhibited Listeria and other lactic acid bacteria (LAB). Leucocin B-TA33a has a predicted molecular mass of 3466 Da, with activity against Leuconostoc/Weissella (W.) strains, and appears similar to mesenterocin 52B and dextranicin 24, while leucocin A-TA33a, which also inhibited Listeria and other LAB strains, is identical to leucocin A-UAL 187. A survey of other known bacteriocin-producing Leuconostoc/Weissella strains for the presence of the three different bacteriocins revealed that production of leucocin A-, B- and C-type bacteriocins
was widespread. Lc. carnosum LA54a, W. paramesenteroides LA7a, and Lc. gelidum UAL 187-22 produced all three bacteriocins, whereas W. paramesenteroides OX and Lc. carnosum TA11a produced only leucocin A- and B-type bacteriocins.
Received: 11 April 1997 / Accepted: 10 June 1997 相似文献
6.
Summary The voltage-dependent sodium channel from the eel electroplax was purified and reconstituted into vesicles of varying lipid composition. Isotopic sodium uptake experiments were conducted with vesicles at zero membrane potential, using veratridine to activate channels and tetrodotoxin to block them. Under these conditions, channel-dependent uptake of isotopic sodium by the vesicles was observed, demonstrating that a certain fraction of the reconstituted protein was capable of mediating ion fluxes. In addition, vesicles untreated with veratridine showed significant background uptake of sodium; a considerable proportion of this flux was blocked by tetrodotoxin. Thus these measurements showed that a significant subpopulation of channels was present that could mediate ionic fluxes in the absence of activating toxins. The proportion of channels exhibiting this behavior was dependent on the lipid composition of the vesicles and the temperature at which the uptake was measured; furthermore, the effect of temperature was reversible. However, the phenomenon was not affected by the degree of purification of the protein used for reconstitution, and channels in resealed electroplax membrane fragments or reconstituted, solely into native eel lipids did not show this behavior. The kinetics of vesicular uptake through these spontaneously-opening channels was slow, and we attribute this behavior to a modification of sodium channel inactivation. 相似文献
7.
8.
Human λ light chain locus: Organization and DNA sequences of three genomicJ regions 总被引:14,自引:0,他引:14
Evidence for the genomic organization of human lambda light chain joining (J) region gene segments is presented. A mouse J probe was used in Southern hybridizations to localize joining region sequences in a cosmid clone containing the genomic cluster of six human lambda constant (C) region gene segments. The results of these hybridizations suggest the presence of at least one J gene segment upstream from each constant region gene segment. The DNA sequences indicate that the human JI, J2, and J3 gene segments have consensus nonamer and heptamer sequences, proposed to be involved in V-J joining, are capable of encoding the known amino acid sequences for the respective J peptides, and have a sequence which could give functional RNA splice site at the end of their coding regions. Our data show that a single functional J is located 1.3 or 1.6 kb upstream of each of the C gene segments known to encode the Mcg, Kern– Oz–, and Kern–Oz+ isotypes. Therefore, the gene organization of this region of the human lambda locus is J1 CI -J2C2-J3C3. The DNA sequences ofJ
1,J
2, andJ
3 presented in this paper establish that a singleJ
gene segment precedes each expressed C gene segment, and support a model for the evolution of the human JC clusters where JICI andJ2C2-J3C3. arose from different ancestral JC units. 相似文献
9.
10.
Stimulation of phosphatidylinositol 4,5-bisphosphate phospholipase C activity by phosphatidic acid 总被引:5,自引:0,他引:5
Phosphatidic acid was a potent activator of the phosphatidylinositol 4,5-bisphosphate (PtdIns-P2) phospholipase C activity associated with human platelet membranes. Lysophosphatidic acid was half as active as phosphatidic acid, and shortening the fatty acid chain reduced the effectiveness of the corresponding phosphatidic acid. Compounds lacking either the phosphate group (diacylglycerol or phorbol ester) or the fatty acid (glycerol phosphate) were not activators. When the negative charge was contributed by a carboxyl group (fatty acid or phosphatidylserine), stimulation of phospholipase C was weak but detectable. Structural analogs of phosphatidic acid (lipopolysaccharide, lipid A, and 2,3-diacylglucosamine 1-phosphate) were less effective but also enhanced PtdIns-P2 hydrolysis. Phosphatidic acid potentiated the activation of phospholipase C by alpha-thrombin, chelators, and guanine nucleotides. Phosphatidylinositol 4-phosphate and PtdIns-P2 were also effective activators of PtdIns-P2 degradation. Other phospholipids were without effect. The production of inositol 1,4,5-trisphosphate and diacylglycerol via the activation of phospholipase C provides a rationale for the cellular responses evoked by phosphatidic acid and the ability of this phospholipid to potentiate and initiate hormonal responses. 相似文献